Vecuronium bromide

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Vecuronium bromide

Vecuronium bromide is a muscle relaxant used in anesthesia to facilitate endotracheal intubation and to provide skeletal muscle relaxation during surgery or mechanical ventilation. It is a non-depolarizing neuromuscular blocking agent of intermediate duration. Vecuronium bromide works by competing with acetylcholine for receptors at the neuromuscular junction, leading to muscle relaxation. It is often preferred in patients with cardiovascular problems due to its minimal effects on heart rate and blood pressure.

Pharmacology[edit | edit source]

Vecuronium bromide acts by binding competitively to the nicotinic acetylcholine receptors at the neuromuscular junction, inhibiting acetylcholine from binding and thus preventing muscle contraction. Its action is reversed by acetylcholinesterase inhibitors, such as neostigmine, which increase the concentration of acetylcholine at the neuromuscular junction.

Indications[edit | edit source]

Vecuronium bromide is indicated for use as an adjunct to general anesthesia to facilitate endotracheal intubation and to provide skeletal muscle relaxation during surgery or mechanical ventilation. It is also used in the ICU setting for managing patients requiring mechanical ventilation.

Dosage and Administration[edit | edit source]

The dosage of vecuronium bromide varies based on the patient's weight, the desired degree of muscle relaxation, and the method of administration. It is typically administered intravenously, and its effects are seen within 2 to 3 minutes of administration.

Side Effects[edit | edit source]

Common side effects of vecuronium bromide include:

  • Skin flushing
  • Hypotension
  • Tachycardia
  • Bronchospasm
  • Anaphylaxis (rare)

Prolonged use of vecuronium bromide can lead to muscle weakness and myopathy, especially in critically ill patients.

Contraindications[edit | edit source]

Vecuronium bromide is contraindicated in patients with known hypersensitivity to the drug. Caution is advised in patients with neuromuscular diseases such as myasthenia gravis, as the effects of vecuronium may be profoundly increased in these individuals.

Pharmacokinetics[edit | edit source]

Vecuronium bromide is metabolized in the liver and excreted by the kidneys. Its elimination half-life is approximately 65 to 75 minutes, but this can be prolonged in patients with hepatic or renal impairment.

History[edit | edit source]

Vecuronium bromide was introduced in the 1980s as a safer alternative to older neuromuscular blocking agents. It quickly gained popularity due to its favorable pharmacokinetic profile and minimal cardiovascular effects.

See Also[edit | edit source]


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Contributors: Prab R. Tumpati, MD